Broadly neutralizing antibodies protect against hepatitis C virus quasispecies challenge

被引:0
|
作者
Mansun Law
Toshiaki Maruyama
Jamie Lewis
Erick Giang
Alexander W Tarr
Zania Stamataki
Pablo Gastaminza
Francis V Chisari
Ian M Jones
Robert I Fox
Jonathan K Ball
Jane A McKeating
Norman M Kneteman
Dennis R Burton
机构
[1] The Scripps Research Institute,Department of Immunology
[2] The Scripps Research Institute,Department of Molecular Biology
[3] The Scripps Research Institute,Departments of Molecular and Experimental Medicine
[4] University of Alberta,Department of Surgery
[5] 2-75 Heritage Medical Research Building,Division of Immunity and Infection
[6] Institute of Infection,undefined
[7] Immunity and Inflammation,undefined
[8] School of Molecular Medical Sciences,undefined
[9] the University of Nottingham,undefined
[10] Queen's Medical Centre,undefined
[11] Institute of Biomedical Research,undefined
[12] Medical School,undefined
[13] University of Birmingham,undefined
[14] School of Biological Sciences,undefined
[15] University of Reading,undefined
[16] Whiteknights,undefined
[17] Rheumatology Clinic,undefined
[18] Scripps Memorial Hospital,undefined
[19] Present address: Calmune Corporation,undefined
[20] Suite 130,undefined
[21] 9393 Towne Center Drive,undefined
[22] San Diego,undefined
[23] California 92121,undefined
[24] USA.,undefined
来源
Nature Medicine | 2008年 / 14卷
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摘要
A major problem in hepatitis C virus (HCV) immunotherapy or vaccine design is the extreme variability of the virus. We identified human monoclonal antibodies (mAbs) that neutralize genetically diverse HCV isolates and protect against heterologous HCV quasispecies challenge in a human liver–chimeric mouse model. The results provide evidence that broadly neutralizing antibodies to HCV protect against heterologous viral infection and suggest that a prophylactic vaccine against HCV may be achievable.
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页码:25 / 27
页数:2
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